Large deletions in the phenylalanine hydroxylase gene as a cause of phenylketonuria in India

Publisher Website

1 November 1997

journal article
Published by Wiley in Journal of Inherited Metabolic Disease

Vol. 20 (6), 845-846
https://doi.org/10.1023/a:1005352725283

Abstract

No abstract available

Keywords

This publication has 2 references indexed in Scilit:

Phenylalanine hydroxylase gene mutations in the United States: report from the Maternal PKU Collaborative Study.
1996
A single origin of phenylketonuria in Yemenite Jews
Nature, 1990

Cited by 7 articles